Total synthesis of diaportheone A |
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Authors: | Mario A. Tan Patrik Peter Züger Silvio Roggo |
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Affiliation: | 1. Research Center for the Natural and Applied Sciences and College of Science, University of Santo Tomas, Espana, Manila 1015, Philippines;2. Institute for Biomedical Research, Novartis Pharma, Basel, Switzerland |
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Abstract: | Diaportheone A (1), a chromone natural product was previously isolated from the endophytic fungi Diaporthe sp. P 133. Its structure was established by spectroscopic methods, however, its absolute configuration remained undefined. This study dealt on the total synthesis of diaportheone A (1) utilizing the cyclization and in situ thermal syn-elimination of a β-ketosulfoxide. The C-1R absolute configuration of the natural product was established by X-ray crystallography of the synthetic diaportheone A (1) (>99%?ee) and comparison with the optical rotation. |
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Keywords: | Chromone Diaportheone X-ray crystallography |
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